Literature DB >> 21341758

The formal [4+3] cycloaddition between donor-acceptor cyclobutanes and nitrones.

Andrew C Stevens1, Cory Palmer, Brian L Pagenkopf.   

Abstract

The formal [4+3] cycloaddition of 2-alkoxy-1,1-dicarboxylate activated donor-acceptor cyclobutanes with nitrones is disclosed. The reaction forms structurally unique oxazepines in moderate to high yield with a wide scope of nitrones. In most cases either a diastereomeric mixture or a single diastereomer may be formed, depending on the reaction conditions.

Entities:  

Year:  2011        PMID: 21341758     DOI: 10.1021/ol200220d

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  2 in total

1.  Reactivity of (Z)-4-Aryliden-5(4H)-thiazolones: [2 + 2]-Photocycloaddition, Ring-Opening Reactions, and Influence of the Lewis Acid BF3.

Authors:  Sonia Sierra; David Dalmau; Sheila Higuera; Darío Cortés; Olga Crespo; Ana I Jimenez; Alexandra Pop; Cristian Silvestru; Esteban P Urriolabeitia
Journal:  J Org Chem       Date:  2021-08-16       Impact factor: 4.198

2.  The Cleavage of a C-C Bond in Cyclobutylanilines by Visible-Light Photoredox Catalysis: Development of a [4+2] Annulation Method.

Authors:  Jiang Wang; Nan Zheng
Journal:  Angew Chem Int Ed Engl       Date:  2015-07-24       Impact factor: 15.336

  2 in total

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